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Human Mutation|December 24, 2002
Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexityNadia A Chuzhanova, Emmanuel J Anassis, Edward V Ball, et al.Human Mutation|December 24, 2002
Sequence diversity of KIAA0027/MLC1: are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?Claudia Rubie, Peter Lichtner, Jutta Gärtner, et al.Human Mutation|December 24, 2002
Dynamics of CAG repeat loci revealed by the analysis of their variabilityAida M Andrés, Oscar Lao, Marta Soldevila, et al.Human Mutation|December 24, 2002
ATM mutations on distinct SNP and STR haplotypes in ataxia-telangiectasia patients of differing ethnicities reveal ancestral founder effectsCatarina Campbell, Midori Mitui, Laura Eng, et al.Human Mutation|December 24, 2002
BRCA1 germline mutations in Indian familial breast cancerMani T Valarmathi, Agarwal A, Suryanarayana S V Deo, et al.Human Mutation|December 24, 2002
Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1Kathrin Huehne, Vladimir Benes, Christian Thiel, et al.Human Mutation|January 29, 2003
Missense mutations in the DNA-binding region and termination codon in PAX6Lian-Yu Chao, Rajnikant Mishra, Louise C Strong, et al.Human Mutation|January 29, 2003
The Iranian Human Mutation Gene Bank: a data and sample resource for worldwide collaborative genetics researchHossein Najmabadi, Maryam Neishabury, Farhad Sahebjam, et al.Human Mutation|January 29, 2003
Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutationSandra Angèle, Anthony Laugé, Marie Fernet, et al.Human Mutation|January 29, 2003
Identification of GUCY2D gene mutations in CORD5 families and evidence of incomplete penetranceNitin Udar, Svetlana Yelchits, Meenal Chalukya, et al.Pageof 577